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Meso-ORIGINS: An observational study investigating the origins of mesothelioma

Meso-ORIGINS: Mesothelioma Observational study of RIsk prediction and Generation of paired benign-meso tissue samples, Including a Nested MRI Sub-study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN22929761
Enrollment
600
Registered
2021-08-13
Start date
2022-06-16
Completion date
Unknown
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with benign asbestos-associated pleural disease and patients with suspected mesothelioma Cancer Malignant neoplasm of lung

Interventions

Arm A will follow patients up over a 2-year period following an initial benign pleural biopsy. All patients will have their initial pleural biopsies retrieved and banked and all will have baseline ris

Sponsors

NHS Greater Glasgow and Clyde
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 120 Years

Inclusion criteria

Inclusion criteria: Arm A: 1. History of asbestos exposure or imaging compatible with this (e.g., pleural plaques) 2. Any form of pleural biopsy within the last 1 year showing evidence of associated pleural inflammation (e.g., benign fibrinous pleurisy, non-specific pleuritis, atypical mesothelial proliferation) 3. Informed written consent (to at least banking of previous and future pleural tissue samples) Arm A MRI sub-study: 1. Registered to Arm A 2. Informed written consent Arm B: 1. Suspected pleural malignancy, defined by a unilateral pleural effusion or mass 2. History of asbestos exposure or typical radiological features, e.g., pleural plaques 3. Sufficient fitness for thoracoscopy (LAT or VATS are permissible) 4. Informed written consent Added 21/08/2025: Arm A and B: =16 years of age

Exclusion criteria

Exclusion criteria: Arm A: 1. Any cytologically or histologically confirmed pleural malignancy 2. Any pleural infection including TB 3. Granulomatous pleural inflammation 4. Any specific pleuritis (e.g., RA) 5. Previous pleurodesis Arm A MRI sub-study: 1. Any contraindication to MRI, e.g., claustrophobia, pregnancy, metallic foreign body, pacemaker/implant 2. Allergy to gadolinium contrast 3. eGFR <30 ml/min Arm B: 1. Current or recent (within the last 3 months) intercostal chest drain 2. Previous pleurodesis

Design outcomes

Primary

MeasureTime frame
Number of patients in Arm A diagnosed with malignant pleural mesothelioma based on histological confirmation in tissue biopsies at any point from study registration to completion of 2 years follow-up

Secondary

MeasureTime frame
1. Results of a multiomic risk classifier based on radiomics based on perfusion MRI early contrast enhancement, proteomic assay to be confirmed, exhaled breath metabolomics by gas chromatography-mass spectrometry at baseline in Arm A 2. Number of patients in the Arm B with histologically confirmed malignant pleural mesothelioma following thoracoscopy

Countries

England, Scotland, United Kingdom, Wales

Contacts

Public ContactAlexandrea MacPherson
alexandrea.macpherson@glasgow.ac.uk+44 (0)141 330 7282

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jul 23, 2026